FDA Inspection 1208833 - NEOSS AB - June 27, 2023

Record Details

This FDA Inspection record concerns NEOSS AB, with an inspection on June 27, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: NEOSS AB
Inspection Date: June 27, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dd592a8f-88a0-4ed3-9ff4-5f3014e0520c

Violation Codes2

21 CFR 820.198(a)21 CFR 820.22

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